Adherence to hydroxyurea medication by children with sickle cell disease (SCD) using an electronic device: a feasibility study
Author:
Funder
Ruth Mott Foundation
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12185-016-2027-x.pdf
Reference27 articles.
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3. Piccin A, Murphy C, Eakins E, Kinsella A, McMahan C, Smith OP, Murphy W. Protein C and free protein S in children with sickle cell anemia. Ann Hematol. 2012;91:1669–71.
4. Strouse JJ, Heeney MM. Hydroxyurea for the treatment of sickle cell disease: efficacy, barriers, toxicity, and management in children. Pediatr Blood Cancer. 2012;59:365–71.
5. Wong TE, Brandow AM, Lim W, Lottenberg R. Update on the use of hydroxyurea therapy in sickle cell disease. Blood. 2014;124:3850–7.
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